Marketed Without An Approved NDA/ANDA: Dietary supplements contains undeclared sibutramine, desmethylsibutramine and phenolphthalein based on FDA sampling.
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📍Recalling firmLife and More LLC5771 NW 112th Ave Apt 112 · Doral, FL 33178-4161
✎ GovInfoNow plain-language explainer
Life and More LLC is recalling Akttive High Performance Fat Burner Gold dietary supplement capsules because they contain undeclared sibutramine, desmethylsibutramine, and phenolphthalein. These substances are not listed on the label and pose health risks associated with unapproved drug ingredients. The recall covers 783 bottles distributed nationwide and in Colombia. Read more at govinfonow.com/recall/44097-life-and-more-llc-recalls-akttive-high-performance-fat-burner.
“Akttive Fat Burner Recall: Undeclared Sibutramine Hazard.” GovInfoNow, updated October 12, 2026. https://govinfonow.com/recall/44097-life-and-more-llc-recalls-akttive-high-performance-fat-burner. Based on FDA recall #D-0664-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0664-2016%22&limit=1).
The FDA announced on July 13, 2015, that Life and More LLC voluntarily recalled Akttive High Performance Fat Burner Gold dietary supplement capsules. The product contains undeclared sibutramine, desmethylsibutramine, and phenolphthalein.
How to tell if you have it
Brand: Akttive
Product: High Performance Fat Burner Gold Capsules
Lot #: 000815004400
Expiration: 12/17
Quantity: 783 bottles
The hazard
The FDA stated the capsules are marketed without an approved New Drug Application or Abbreviated New Drug Application because they contain undeclared sibutramine, desmethylsibutramine, and phenolphthalein based on FDA sampling.
Context
GovInfoNow's records show other recent recalls of similar products include StuffbyNainax MR 7 SUPER 700000 Capsules (2025-12-15) and Alembic Fesoterodine Tablets Recall (2025-12-16). Sun Pharmaceutical Carbamazepine Tablets Recall occurred on 2026-08-03.
How to tell if you have this one
Look for a 30-count bottle of Akttive High Performance Fat Burner Gold capsules. Check the label for Lot # 000815004400 and an expiration date of 12/17. The product was distributed by Life and More, L.L.C. of Doral, Florida.
Brand
Akttive
Category
Drug
Based on the official FDA remedy
What to do — step by step
Stop Using the Product
Discontinue use of the recalled Akttive High Performance Fat Burner Gold capsules immediately due to the presence of undeclared drug ingredients.
Discard or Return the Product
The recall record does not specify a return address or disposal method, so consumers should dispose of the product safely and check with the distributor for further instructions.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Nationwide and Colombia, South America” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 7 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #D-0664-2016 (July 13, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0664-2016 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 12, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.